Department of Physiology and Pathophysiology, Peking University Health Science Center and Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Beijing 100191, China.
Department of Surgery, University of Michigan Medical Center, Ann Arbor, MI 48109, USA.
Sci Rep. 2016 Nov 8;6:34747. doi: 10.1038/srep34747.
Nesfatin-1, an 82 amino acid gastric peptide, is involved in regulation of food uptake and in multiple metabolic activities. Whether nesfatin-1 modulates the differentiation and lipid metabolism of brown adipocytes remains unknown. In the present study, we found that nesfatin-1 mRNA and protein were detectable in isolated brown adipocytes and gradually decreased during differentiation (95% CI 0.6057 to 1.034, p = 0.0001). The decrease in nesfatin-1 was associated with a significant reduction in p-S6. Exposure to nesfatin-1 promoted differentiation of brown adipocytes as revealed by a significant increase in UCP1 mRNA (p = 0.03) and lipolysis-related ATGL mRNA (p = 0.04). Nesfatin-1 attenuated phosphorylation of S6K and S6 during brown adipocyte differentiation. Activation of mTOR by leucine or deletion of TSC1 decreased expression of brown adipocyte-related genes UCP1, UCP3, PGC1α and PRDM16, as well as COX8B and ATP5B. Both leucine and TSC1 deletion blocked nesfatin-1-induced up-regulation of UCP1, PGC1α, COX8B and ATP5B in differentiated brown adipocytes. In conclusion, nesfatin-1 promotes the differentiation of brown adipocytes likely through the mTOR dependent mechanism.
nesfatin-1 是一种 82 个氨基酸的胃肽,参与食物摄取和多种代谢活动的调节。nesfatin-1 是否调节棕色脂肪细胞的分化和脂质代谢尚不清楚。在本研究中,我们发现 nesfatin-1 mRNA 和蛋白可在分离的棕色脂肪细胞中检测到,并在分化过程中逐渐降低(95%CI 0.6057 至 1.034,p=0.0001)。nesfatin-1 的减少与 p-S6 的显著减少相关。nesfatin-1 的暴露促进了棕色脂肪细胞的分化,这表现为 UCP1 mRNA 的显著增加(p=0.03)和与脂肪分解相关的 ATGL mRNA 的增加(p=0.04)。nesfatin-1 减弱了 S6K 和 S6 在棕色脂肪细胞分化过程中的磷酸化。亮氨酸激活 mTOR 或 TSC1 缺失会降低与棕色脂肪细胞相关的基因 UCP1、UCP3、PGC1α 和 PRDM16 以及 COX8B 和 ATP5B 的表达。亮氨酸和 TSC1 缺失均阻断了 nesfatin-1 诱导的分化棕色脂肪细胞中 UCP1、PGC1α、COX8B 和 ATP5B 的上调。总之,nesfatin-1 可能通过 mTOR 依赖的机制促进棕色脂肪细胞的分化。